1. Volume 107, Issue 10, Pages 2253-2262 (November 2014)
A Raman Microspectroscopy Study of Water and Trehalose in Spin-Dried Cells 
Alireza Abazari, Nilay Chakraborty, Steven Hand, Alptekin Aksan, Mehmet Toner 
Biophysical Journal 
Volume 107, Issue 10, Pages (November 2014)
DOI: /j.bpj
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2. Figure 1
Raman scattering spectra collected from (a) dry cell lysate, (b–e) mixtures of cell lysate/trehalose at ratios of 1:1, 1:2, 1:4, and 1:10 g trehalose/g dry weight. Inset: blow-up of the region 720–1800 cm−1. Annotations – 1), 851 cm−1 (saccharides, trehalose), 2), 920 cm−1 (C-C stretch of saccharides), 3), 1583 cm−1 (attributed to C=C stretch in L-tryptophan, various nucleic acids, guanine, phenylalanine), 4), 1667 cm−1 (protein band, Amide I), 5), ∼2940 cm−1 (C-H stretch of organic matter), 6), 3250–3350 cm−1 (O–H symmetric stretch low energy band), 7), 3350–3500 cm−1 (O–H antisymmetric stretch high energy band).
Biophysical Journal  , DOI: ( /j.bpj )
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3. Figure 2
(A) Ratio of the Raman intensity of the peak at 1667 cm−1, representing proteins, to the C-H stretch peak intensity at 2940 cm−1, representing all the organic matter, at various LYS/TRE ratios against water content. (B) Calibration curve for (trehalose/protein) ratio based on intensity ratio of 851 cm−1 to 1667 cm−1 in oven-dried (0 g water/g dry weight) samples. (C) Ratio of O-H stretch intensities at 3430 cm−1 to 3300 cm−1 at various LYS/TRE ratios against water content (Inset: The intensity ratio 3430 cm−1 to 3300 cm−1 for nitrogen-dried samples plotted against TRE/LYS ratios. Dashed line denotes the background intensity not from water). (D) Ratio of the O-H stretch intensity at 3430 cm−1 to that of C-H stretch at 2940 cm−1 at various LYS/TRE ratios against water content.
Biophysical Journal  , DOI: ( /j.bpj )
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4. Figure 3
(A1 and A2) Brightfield images of C3A and TRET cells, embedded in a trehalose layer after spin-coating and desiccation under nitrogen flow. The white dotted line represents the XZ plane of scan. (B) Area-averaged intracellular spectrum collected from C3A and TRET cells. (C) Area-averaged spectra collected from the extracellular thin layer of trehalose.
Biophysical Journal  , DOI: ( /j.bpj )
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5. Figure 4
Reconstructed confocal Raman images of C3A (A1–A3) and TRET (B1–B3) cells, based on protein (row 1), trehalose (row 2), and O-H stretch (row 3) contrasts. Images show cross sections of cells in the XZ plane, with air at the top and CaF2 substrate at the bottom. The thin gray lines constitute the approximate boundaries of the cells (C1–C3) Respective distributions of proteins, trehalose, and O-H stretch across the cell width along the thick dashed white line. (D and E) Estimated amount of trehalose/protein and water/dry weight ratios from I851/I1667 and I3300/I2940 ratios, respectively.
Biophysical Journal  , DOI: ( /j.bpj )
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